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静脉注射丙戊酸钠与地塞米松治疗急性偏头痛的疗效比较:一项双盲随机临床试验

Effect of intravenous sodium valproate vs dexamethasone on acute migraine headache: a double blind randomized clinical trial.

作者信息

Mazaheri Shahir, Poorolajal Jalal, Hosseinzadeh Akram, Fazlian Mohammad Mahdi

机构信息

Department of Neurology, School of Medicine, Hamadan University of Medical Sciences, Hamadan, Iran.

Modeling of Noncommunicable Diseases Research Center and Department of Epidemiology & Biostatistics, School of Public Health, Hamadan University of Medical Sciences, Hamadan, Iran.

出版信息

PLoS One. 2015 Mar 20;10(3):e0120229. doi: 10.1371/journal.pone.0120229. eCollection 2015.

Abstract

BACKGROUND

Despite the impact of sodium valproate and dexamethasone on migraine headache, the efficacy of the two drugs has not been properly investigated and compared. This trial compared the effect of the two drugs on acute migraine headache.

METHODS

This double blind randomized clinical trial was conducted on patients aged 18 to 65 years with acute migraine headache who referred to the emergency departments of Beasat and Farshchian Hospitals in Hamadan, Iran, from April 2012 to June 2014. Patients were randomly assigned to receive a single-dose of either 400 mg sodium valproate or 16 mg dexamethasone plus 50 ml saline normal solution within 15 min intravenously. The severity of headache in the two groups was evaluated at baseline, 0.5 and 2 hours later using the Visual Analog Scale (VAS) on a scale of 0 to 10.

RESULTS

Of 104 patients enrolled, 72 patients remained for analysis. The effect of both sodium valproate and dexamethasone on acute migraine headache was statistically significant at 0.5 and 2 hours post-treatment compared to pre-treatment (P=0.001). The severity of headache based on VAS reduced form 8.20 (7.72, 8.68) before treatment to 5.31 (4.74, 5.89) and 3.66 (2.99, 4.33) at 0.5 and 2 hours after treatment, respectively, in patients receiving sodium valproate and from 8.46 (8.05, 8.86) before treatment to 5.46 (4.81, 6.11) and 3.59 (2.84, 4.35) at 0.5 and 2 hours after treatment, respectively, in patients receiving dexamethasone. Both drugs were highly effective in improvement of acute headache in patients without aura. However, sodium valproate significantly improved the acute headache in patients with aura but dexamethasone did not. The severity of headache based on VAS reduced form 8.50 (7.40, 9.60) before treatment to 4.67 (2.40, 6.93) and 3.50 (1.78, 5.22) at 0.5 and 2 hours after treatment, respectively, in patients with aura receiving sodium valproate and from 8.80 (7.76, 9.84) before treatment to 7.20 (4.98, 9.42) and 6.20 (2.43, 9.97) at 0.5 and 2 hours after treatment, respectively, in patients with aura receiving dexamethasone.

CONCLUSIONS

This trial indicated that, in overall, intravenous sodium valproate is not superior to intravenous dexamethasone in treatment of acute migraine attacks. However, in patients with aura, only sodium valproate but not dexamethasone is effective in headache relief. This issue needs further investigations.

TRIAL REGISTRATION

ClinicalTrials.gov IRCT201202199014N1.

摘要

背景

尽管丙戊酸钠和地塞米松对偏头痛有影响,但这两种药物的疗效尚未得到充分研究和比较。本试验比较了这两种药物对急性偏头痛的疗效。

方法

本双盲随机临床试验于2012年4月至2014年6月在伊朗哈马丹的贝萨特医院和法尔什恰安医院急诊科就诊的18至65岁急性偏头痛患者中进行。患者被随机分配在15分钟内静脉注射单剂量400毫克丙戊酸钠或16毫克地塞米松加50毫升生理盐水。两组患者在基线、0.5小时和2小时后使用视觉模拟量表(VAS)(范围为0至10)评估头痛严重程度。

结果

在纳入的104例患者中,72例患者留作分析。与治疗前相比,丙戊酸钠和地塞米松对急性偏头痛的疗效在治疗后0.5小时和2小时均具有统计学意义(P = 0.001)。接受丙戊酸钠治疗的患者,基于VAS的头痛严重程度从治疗前的8.20(7.72,8.68)分别降至治疗后0.5小时的5.31(4.74,5.89)和2小时的3.66(2.99,4.33);接受地塞米松治疗的患者,从治疗前的8.46(8.05,8.86)分别降至治疗后0.5小时的5.46(4.81,6.11)和2小时的3.59(2.84,4.35)。两种药物对无先兆患者的急性头痛改善均非常有效。然而,丙戊酸钠能显著改善有先兆患者的急性头痛,而地塞米松则不能。接受丙戊酸钠治疗的有先兆患者,基于VAS的头痛严重程度从治疗前的8.50(7.40,9.60)分别降至治疗后0.5小时的4.67(2.40,6.93)和2小时的3.50(1.78,5.22);接受地塞米松治疗的有先兆患者,从治疗前的8.80(7.76,9.84)分别降至治疗后0.5小时的7.20(4.98,9.42)和2小时的6.20(2.43,9.97)。

结论

本试验表明,总体而言,静脉注射丙戊酸钠在治疗急性偏头痛发作方面并不优于静脉注射地塞米松。然而,在有先兆的患者中,只有丙戊酸钠对缓解头痛有效,而地塞米松无效。这个问题需要进一步研究。

试验注册

ClinicalTrials.gov IRCT201202199014N1。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e13/4368536/09a277a26662/pone.0120229.g001.jpg

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